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5,534 Possible Causes for Jaundice, Non-Hemolytic Unconjugated Hyperbilirubinemia, Psychomotor Development Delayed

  • Gilbert Syndrome

    The role of GS in neonatal jaundice is unknown.[ncbi.nlm.nih.gov] Constitutional liver dysfunction Familial non-hemolytic non-obstructive jaundice Icterus intermittens juvenilis Low-grade chronic hyperbilirubinemia Unconjugated benign bilirubinemia[en.wikipedia.org] Tagged as: constitutional liver dysfunction, familial benign unconjugated hyperbilirubinaemia, familial non-hemolytic non-obstructive jaundice, Gilbert–Meulengracht syndrome[highrisklifeinsuranceagency.com]

    Missing: Psychomotor Development Delayed
  • Crigler-Najjar Syndrome Type 1

    Clinically apparent jaundice is unusual in patients with beta-thalassemia major.[ncbi.nlm.nih.gov] Mutations in the UGT1A1 gene cause Crigler-Najjar syndrome (CN), which causes non-hemolytic unconjugated hyperbilirubinemia, and is categorized as CN1 and CN2 according to[ncbi.nlm.nih.gov] Crigler-Najjar (CN) syndrome is a rare autosomal recessive inherited disorder characterized by non-hemolytic, unconjugated hyperbilirubinemia.[ncbi.nlm.nih.gov]

    Missing: Psychomotor Development Delayed
  • Early Infantile Epileptic Encephalopathy Type 6

    In the absence of jaundice, splenomegaly, or complications the disease may remain undetected.[centogene.com] We report on a patient who developed, from 5 months of age, multiple seizure types, including myoclonic, associated with severe psychomotor delay, leading to the diagnosis[ncbi.nlm.nih.gov] More severe liver injury can cause nausea, vomiting, abdominal pain, fatigue, anorexia, jaundice and/or dark urine.[fda.gov]

  • Brandt Syndrome

    Symptoms may include: Fatigue Yellowing of the skin and whites of the eyes (mild jaundice) In people with Gilbert syndrome, jaundice most often appears during times of exertion[medlineplus.gov] This is a symptom of jaundice . Jaundice usually appears within 20 days after the onset of symptoms.[healthline.com] When infantile papular acrodermatitis is caused by hepatitis B, there may be an enlarged liver, but there is seldom any jaundice .[dermnetnz.org]

  • Citrullinemia

    Three patients with infantile cholestatic jaundice were found to have mutations of the SLC25A13 gene.[ncbi.nlm.nih.gov] Abstract We describe 2 patients with adult-onset type II citrullinemia who developed transient hypoproteinemia and jaundice in early infancy.[ncbi.nlm.nih.gov] Elevated aminotransferases, jaundice, an elevated international normalized ratio, and confusion were typical of idiopathic ALF, and a low serum ceruloplasmin level initially[nucdf.org]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Neonatal Adrenoleukodystrophy

    Hepatic dysfunction is first displayed in infants with jaundice and later in some with episodes of intracranial bleeding due to vitamin K-responsive coagulopathy.[orpha.net] Psychomotor development is delayed, but children are usually able to walk and say a few words.[rarediseases.info.nih.gov] psychomotor development.[ela-asso.com]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Massive Hepatic Necrosis

    Cook GC, Sherlock S: Jaundice and its relation to therapeutic agents.[link.springer.com] Gilbert’s Disease Chronic, benign, intermittent, familial (AD), non-hemolytic unconjugated hyperbilirubinemia with evanescent increases of B1 Due to defective transport and[slideshare.net] Jaundice tnetic Shock 1 Noted to be Jaundiced on day he died 1 Hal 44 Jaundiced last day of life 1 3 Hal 74 History of hepatic disease 9 1 Cyclo 185 Jaundiced last day 1 2[nap.edu]

    Missing: Psychomotor Development Delayed
  • Thalassemia

    Diagnostic methods Diagnosis is suspected in infants younger than 2 years of age with severe microcytic anemia, mild jaundice and hepatosplenomegaly.[orpha.net] psychomotor development, intellectual disability, and characteristic facial features (summary by O'Rawe et al., 2015).[ncbi.nlm.nih.gov] Clinical description Patients present with moderate to severe anemia, jaundice and splenomegaly.[orpha.net]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Fetal Erythroblastosis

    They can range from mild anemia and jaundice to fetal death in utero .[medindia.net] In a second case, delayed speech development was observed.[ncbi.nlm.nih.gov] […] in the blood of an Rh-positive fetus which cross the placenta and destroy fetal erythrocytes and that is characterized by an increase in circulating erythroblasts and by jaundice[merriam-webster.com]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia
  • Cytomegalovirus Infection

    RATIONALE: Septo-optic dysplasia (SOD) is a rare congenital disorder that may cause jaundice in infants.[ncbi.nlm.nih.gov] psychomotor development.[nejm.org] Anamnesis offered reliable diagnostic criteria for intrauterine infection (flu during first trimester of pregnancy, intrauterine growth restriction, prolonged jaundice).[ncbi.nlm.nih.gov]

    Missing: Non-Hemolytic Unconjugated Hyperbilirubinemia

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